methotrexate

Generic: methotrexate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methotrexate
Generic Name methotrexate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methotrexate sodium 2.5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-136
Product ID 82804-136_a76808f0-38a7-4b54-a4fb-3584f9058ae5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213343
Listing Expiration 2026-12-31
Marketing Start 2020-08-24

Pharmacologic Class

Classes
folate analog metabolic inhibitor [epc] folic acid metabolism inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804136
Hyphenated Format 82804-136

Supplemental Identifiers

RxCUI
105585
UPC
0382804136308
UNII
3IG1E710ZN

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methotrexate (source: ndc)
Generic Name methotrexate (source: ndc)
Application Number ANDA213343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-136-30)
source: ndc

Packages (1)

82804-136-30 30 TABLET in 1 BOTTLE (82804-136-30)

Ingredients (1)

methotrexate sodium (2.5 mg/1)

Linked Drug Pages (1)

Methotrexate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a76808f0-38a7-4b54-a4fb-3584f9058ae5", "openfda": {"upc": ["0382804136308"], "unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["a76808f0-38a7-4b54-a4fb-3584f9058ae5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-136-30)", "package_ndc": "82804-136-30", "marketing_start_date": "20240828"}], "brand_name": "Methotrexate", "product_id": "82804-136_a76808f0-38a7-4b54-a4fb-3584f9058ae5", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "82804-136", "generic_name": "Methotrexate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA213343", "marketing_category": "ANDA", "marketing_start_date": "20200824", "listing_expiration_date": "20261231"}